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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K152864
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Product Description
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Recall
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FDA Recall
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Merge Hemo, Software packages 10.2, 10.3, and 10.4 2 08/28/2021 Merge Healthcare, Inc.
Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power strip (PS-415-HGULTRA - ... 2 01/14/2018 Merge Healthcare, Inc.
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